用于疫苗开发中多价抗原递送的自组装蛋白纳米粒子平台

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Hao Wu , Ruiqi Weng , Jiaxuan Li , Zhiwei Huang , Xiaotian Tie , Jianhua Li , Keda Chen
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引用次数: 0

摘要

纳米颗粒疫苗可以高效、重复地展示多价抗原,从而提高抗原的靶向递送,诱导更持久的免疫反应,是新型疫苗的重要代表。全球COVID-19大流行加速了纳米颗粒疫苗的开发,为预防和控制传染病提供了一个有希望的解决方案。目前,纳米颗粒疫苗的开发涉及使用各种类型的纳米颗粒,包括脂质体、聚合物、无机材料和乳液。蛋白质纳米颗粒候选疫苗因其独特的抗原呈递方法和开发过程中的自组装特性而越来越受到人们的关注,并对其前景取得了广泛共识。天然自组装的蛋白质纳米颗粒,如铁蛋白,增强抗原呈递,这有助于激活体液和细胞免疫反应。这使得乙型肝炎病毒的研究取得了重大进展。同时,一些合成工程蛋白纳米颗粒如mi3、I53-50通过与SpyTag-SpyCatcher系统的化学偶联可诱导更高的抗体滴度,从而提供更好的免疫保护,在预防H1N1和H3N2流感病毒感染方面具有广阔的应用前景。本文综述了蛋白质纳米颗粒作为抗原递送平台的独特优势、免疫设计机制的进展、相关佐剂在临床前和临床试验中的应用进展,以及常用的计算设计蛋白质纳米颗粒在临床前试验中的表现,重点介绍了阳离子纳米颗粒疫苗的应用进展。目的是为未来的研究人员提供有效的佐剂策略和高质量的计算设计蛋白质纳米颗粒的选择,从而促进蛋白质纳米颗粒疫苗的临床试验进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Self-Assembling protein nanoparticle platform for multivalent antigen delivery in vaccine development

Self-Assembling protein nanoparticle platform for multivalent antigen delivery in vaccine development
Nanoparticle vaccines can efficiently and repeatedly display multivalent antigens, thereby improving the targeted delivery of antigens and inducing more durable immune responses, making them an important representative of novel vaccines. The global COVID-19 pandemic has accelerated the development of nanoparticle vaccines, offering a promising solution for the prevention and control of infectious diseases. Currently, the development of nanoparticle vaccines involves the use of various types of nanoparticles, including liposomes, polymers, inorganic materials, and emulsions. Protein nanoparticles candidate vaccines are attracting increasing attention because of their unique antigen presentation methods and self-assembly characteristics during their development, leading to a broad consensus on their promising future. Naturally self-assembling protein nanoparticles, such as ferritin, enhance antigen presentation, which aids in the activation of both humoral and cellular immune responses. This has led to significant advancements in the study of hepatitis B virus. Meanwhile, some synthetically engineered protein nanoparticles, such as mi3, and I53-50, can induce higher antibody titers through chemical conjugation with the SpyTag-SpyCatcher system, thereby providing better immunoprotection and showing promising prospects in the prevention of H1N1 and H3N2 influenza virus infections. This article reviews the unique advantages of protein nanoparticles as antigen delivery platforms, progress made in immunological design mechanisms, advances in the application of related adjuvants in preclinical and clinical trials, and the performance of commonly used computationally designed protein nanoparticles in preclinical trials, with a particular emphasis on the progress in the application of cationic nanoparticle vaccines. The aim is to provide future researchers with effective adjuvant strategies and high-quality selections for computationally designed protein nanoparticles, thereby promoting the clinical trial process of protein nanoparticles vaccines.
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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